Location: United States-North America – US Home-Based
Job responsibilities
- Development of protocols for clinical studies.
- Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans
- Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Clinical Study Reports, Annual Reports and other Health Authority submissions.
- Monitor, review and summarize safety and efficacy data in ongoing studies.
- Represent clinical development on project teams.
- Clinical lead for study abstracts, posters, oral presentations and manuscripts for assigned studies.
- Serve as liaison to project teams, CRO’s, Clinical sub-teams, and others.
- Maintain updated knowledge of competitive landscape in regard to assets with similar MOA and/or evolving standards of care for indications of interest.
Qualifications
What we’re looking for
- Degree in scientific/life-sciences field. Pharm.D. or Ph.D. preferred.
- Minimum of 8 years of experience in drug development with at least 5 years as clinical research scientist in oncology are required. Hematology experience preferred but not required.
- Strong ability to manage time and work independently.
- Must demonstrate good computer skills especially in the utilization of Microsoft Word, Excel, PowerPoint, and Acrobat software; ability to embrace new technologies.
- Excellent communication, presentation, interpersonal skills, both written and spoken (English required), with an ability to inform, influence, convince, and persuade.
- Flexibility and the ability to mentor and/or manage new staff and to handle multiple tasks to meet deadlines delivering high quality work in a dynamic environment.
Apply here: https://www.syneoshealth.com/clinical-corporate-careers/jobs/14141863-principal-clinical-research-scientist